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The ezetimibe controversy: implications for clinical practice

机译:依泽替米贝争议:对临床实践的启示

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Low-density lipoprotein cholesterol (LDL-C) remains the primary target of lipid-lowering therapy. Achieving LDL-C goals as outlined by the National Cholesterol Education Program Adult Treatment Panel III can be difficult with statins alone; therefore, adjunctive therapy is often indicated to reduce cardiovascular risk. Ezetimibe, a potent inhibitor of intestinal cholesterol absorption, has been shown to be safe, tolerable and effective at lowering LDL-C, non-high-density lipoprotein cholesterol and apolipoprotein B, each of which has been correlated with improved clinical outcomes, alone or in combination with a statin. However, because of randomized trials that demonstrated mixed results about atherosclerotic plaque regression via carotid intima-media thickness and a concern about cancer risk, ezetimibe′s role in lipid therapy has been questioned. Currently, a large randomized controlled trial is in progress to answer if ezetimibe improves clinical outcomes in patients with high-risk acute coronary syndrome. A smaller trial in patients with chronic kidney disease demonstrated reduced clinical events, including myocardial infarction, stroke and revascularization for patients taking the combination of ezetimibe and simvastatin versus those taking statin or placebo alone. In this paper, we review the trials that have led to the ezetimibe controversy and then discuss the possible role of ezetimibe in specific patient populations until the results of ongoing clinical trials are known.
机译:低密度脂蛋白胆固醇(LDL-C)仍然是降脂治疗的主要目标。仅使用他汀类药物就难以实现国家胆固醇教育计划成人治疗小组III概述的LDL-C目标。因此,辅助治疗通常被认为可以降低心血管疾病的风险。依泽替米贝是一种有效的肠道胆固醇吸收抑制剂,已被证明在降低LDL-C,非高密度脂蛋白胆固醇和载脂蛋白B方面是安全,可耐受和有效的,无论是单独使用还是单独使用,它们均与改善临床疗效相关与他汀类药物合用。但是,由于随机试验显示出通过颈动脉内膜-中膜厚度对动脉粥样硬化斑块消退的混合结果以及对癌症风险的关注,因此对依泽替米贝在脂质治疗中的作用提出了质疑。目前,一项大规模的随机对照试验正在进行中,以回答依泽替米贝是否可以改善高危急性冠状动脉综合征患者的临床结局。一项较小的慢性肾脏病患者试验显示,与单独服用他汀类药物和安慰剂的患者相比,服用依泽替米贝和辛伐他汀联合治疗的患者减少了临床事件,包括心肌梗塞,中风和血运重建。在本文中,我们回顾了引起ezetimibe争议的试验,然后讨论了ezetimibe在特定患者人群中的可能作用,直到正在进行的临床试验结果已知为止。

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